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"Stryker" medical light source machine - Taiwan Registration a9442465b88f509129f2ae70ac39c8ae

Access comprehensive regulatory information for "Stryker" medical light source machine in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a9442465b88f509129f2ae70ac39c8ae and manufactured by STRYKER ENDOSCOPY. The authorized representative in Taiwan is STRYKER FAR EAST INC. TAIWAN BRANCH (USA).

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including STRYKER ENDOSCOPY, and 2 recent registrations in the same category. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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a9442465b88f509129f2ae70ac39c8ae
Registration Details
Taiwan FDA Registration: a9442465b88f509129f2ae70ac39c8ae
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Device Details

"Stryker" medical light source machine
TW: "ๅฒ่ณฝๅ…‹"้†ซ็”จๅ…‰ๆบๆฉŸ
Risk Class 2
Cancelled

Registration Details

a9442465b88f509129f2ae70ac39c8ae

DHA00601131700

Company Information

United States

Product Details

For details, it is Chinese approved copy of the imitation order

I General, Plastic Surgery and Dermatology

import

Dates and Status

May 13, 2005

May 13, 2020

Jun 18, 2020

Cancellation Information

Logged out

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